Experience

ALTOGEN SWITZERLAND

• Switzerland
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Consulting Engineer for Novartis

  • Jul 2020 - Present

  • Novartis ARD - Analytical Expert (for ALTOGEN SWITZERLAND)

• Consulting Engineer

  • Jul 2020 - Present



Eurofins

• Luxembourg
• Biotechnology Research
• 700 & Above Employee

• Senior Analyst HPLC (Method developpement and QC)

  • Sep 2016 - Mar 2020

  • Development and validation of analytical methods for API and degradation products by HPLC-UV / UPLC-UV / Ionic chromatography, • In charge for routine analysis within the schedule, • SOP writing in order to optimize the analysis time (yield and efficiency improved), • HPLC Troubleshooting and maintenance (OQ-PQ) (Agilent, Waters, Ionic (Thermo)), • HPLC training for new employees. • Development and validation of analytical methods for API and degradation products by HPLC-UV / UPLC-UV / Ionic chromatography, • In charge for routine analysis within the schedule, • SOP writing in order to optimize the analysis time (yield and efficiency improved), • HPLC Troubleshooting and maintenance (OQ-PQ) (Agilent, Waters, Ionic (Thermo)), • HPLC training for new employees.



Cenexi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Analytical Chemist

  • Jun 2015 - Feb 2016

  • Stability studies for commercial products (full specification analysis) • Data review (HPLC) • Stability studies for commercial products (full specification analysis) • Data review (HPLC)



Celabor scrl

• Belgium
• Research Services
• 1 - 100 Employee

• Analytical Project Leader (Task officer)

  • Aug 2012 - Jun 2013

  • Research, Development and validation of analytical methods by UPLC-MS/MS for API extracted from plants. • Project management • SOP, report and specification writing. • Routine analysis (Ortis, Oxylent SA …) - QC review. • Research, Development and validation of analytical methods by UPLC-MS/MS for API extracted from plants. • Project management • SOP, report and specification writing. • Routine analysis (Ortis, Oxylent SA …) - QC review.



University of Liège

• Belgium
• Higher Education
• 700 & Above Employee

• Analytical chemistry Engineer

  • Oct 2010 - Feb 2012

  • Cidofovir assay in multiple galenic formulations (created by Pharmaceutical Technology Laboratory (sponges, creams, gels)). • Assay, degradation products and preservatives assays for cidofovir stability studies. - SPE « home-made » cartridges to extract cidofovir from urine. - Data analysis with Stab.e.lity® and E.Noval® softwares. Validation report writing. • Method validations and report writing for AFMPS (Belgium Health Authorities) • Routine analysis for enterprises (SGS Lab. Simon, Prométhéra Biosciences, Cardio3 Biosciences, OdysseaPharma, Mithra Pharmaceuticals…) and QC manager. • Impurities scanning by IR. Show less



University of Liège

• Belgium
• Higher Education
• 700 & Above Employee

• Student Internship (Master 2)

  • Mar 2010 - Aug 2010

  • Validation de méthodes pour le dosage de composés pharmaceutiques selon la Pharmacopée Européenne et l’USP. • Adaptation-développement des méthodes de la Pharmacopée Européenne pour les formulations pharmaceutiques. • Analyse des données grâce au logiciel E.Noval® d’Arlenda® et rédaction des rapports de validation. • Rédaction de SOP pour l’utilisation du spectrophotométre d’absorption atomique Varian®. • Qualification d’appareillages HPLC (Waters®, Merck®). • Validation de méthodes pour le dosage de composés pharmaceutiques selon la Pharmacopée Européenne et l’USP. • Adaptation-développement des méthodes de la Pharmacopée Européenne pour les formulations pharmaceutiques. • Analyse des données grâce au logiciel E.Noval® d’Arlenda® et rédaction des rapports de validation. • Rédaction de SOP pour l’utilisation du spectrophotométre d’absorption atomique Varian®. • Qualification d’appareillages HPLC (Waters®, Merck®).